US5190951AExpiredUtility

Quinoline derivatives

63
Assignee: SS PHARMACEUTICAL COPriority: Oct 19, 1990Filed: Oct 9, 1991Granted: Mar 2, 1993
Est. expiryOct 19, 2010(expired)· nominal 20-yr term from priority
A61P 25/02A61P 25/28C07D 401/06C07D 221/16C07D 471/04C07D 219/06A61P 21/00C07D 401/04
63
PatentIndex Score
15
Cited by
8
References
3
Claims

Abstract

Quinoline derivatives of the formula, ##STR1## wherein > A represents a group >N--(CH 2 ) n --, >C═, >C═CH(CH 2 ) n --, or >CH(CH 2 ) n --, wherein n is an integer of 0-7; Y represents a group >C═O or >CHOH, R 1 is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or an alkylthio group, R 2 is a hydrogen atom, a halogen atom, an alkyl group, a hydroxy group, an alkoxy group, a phenyl group which may have a substituent, a phenoxy group, an alkanoyloxy group, or an amino group which may have a substituent, R 3 is a hydrogen atom, a halogen atom, an alkyl group, or an alkoxy group, and m is an integer of 1-3. The compounds and their salts exhibit a superior antiacetylcholinesterase activity with no side effects and are effective for the prevention or cure of senile dementia or memory disturbance.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A quinoline compound represented by the following formula (I): ##STR12## wherein >A- represents a group >N-(CH 2 ) n  -, wherein n is an integer of 0-7; Y represents a group >C=O or >CHOH, R 1  is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or an alkylthio group, R 2  is a hydrogen atom, a halogen atom, an alkyl group, a hydroxy group, an alkoxy group, a phenyl group which may have a substrtuent, a phenoxy group, an alkanoyloxy group, or an amino group which may have a substituent, R 3  is a hydrogen atom, a halogen atom, an alkyl group, or an alkoxy group, and m is an integer of 1-2; or a salt thereof. 
     
     
       2. A composition for inhibiting acetylcholinesterase comprising the quinoline compound or its salt as defined in claim 1 and a pharmaceutically acceptable carrier. 
     
     
       3. A method for treating dementia comprising administering an effective dose of the quinoline compound or its salt as defined in claim 1 to a subject suffering from or under the risks of suffering from dementia.

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